Ageing Clinical Trial
Official title:
Effects of Isoflavone Combined With Astaxanthin on Skin Aging
Verified date | June 2016 |
Source | Seoul National University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Korea: Ministry of Food and Drug Safety |
Study type | Interventional |
Photoaging is caused by the superposition of chronic ultraviolet (UV)-induced damage on the
intrinsic aging process, and accounts for the majority of age-associated changes in skin
appearance. Reactive oxygen species (ROS) play a key role in UV-induced skin damage and
diminish skin matrix protein levels, leading skin aging. Strategies utilizing endogenous
skin antioxidants as well as plant-derived or synthetic compounds have been examined.
Astaxanthin mainly from marine algae and crustaceans is a kind of carotenoids which were
well-known photo-protective agents with strong antioxidant activity. Several studies have
revealed that supplementation of astaxanthin effectively protect skin against UV damage
through free radicals.
In addition, matrix metalloproteinase-1 induced by UV irradiation is an important step
toward skin aging. Recently, many studies pointed out that phytoestrogens exhibit agonistic
and antagonistic estrogen activities, suppressing activity of MMP-1 in skin. Isoflavone is a
kind of phytoestrogen from soybean and mainly act on skin and bones, inhibiting MMP-1
effectively.
The present study is designed to take isoflavone combined with astaxanthin to maximize their
anti-aging ability and objectively measure the effects of the mixture on facial wrinkles,
hydration, and elasticity.
Status | Completed |
Enrollment | 90 |
Est. completion date | December 2015 |
Est. primary completion date | November 2015 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Female |
Age group | 45 Years and older |
Eligibility |
Inclusion Criteria: - Healthy females aged = 45 years - Facial wrinkle grade 2 to 4 Exclusion Criteria: - received medical or cosmetic treatment that interferes with the general aging process at least 3 months before the study - received any hormone replacement therapy at least 3 months before the study - reported taking functional foods more than 1 month during last 3 months before the study - history of acute or chronic disease such as severe liver or kidney disease - history of allergies against any component of trial foods - any visible skin disease that might be confused with a skin reaction to the test procedure |
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Korea, Republic of | Seoul National University Hospital | Seoul |
Lead Sponsor | Collaborator |
---|---|
Seoul National University Hospital |
Korea, Republic of,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change from baseline in skin wrinkles | Facial wrinkles in the crow's feet area measured by Skin Visiometer | Twenty-four weeks | No |
Secondary | Change from baseline in skin elasticity | Facial elasticity measured by Cutometer | Twenty-four weeks | No |
Secondary | Change from baseline in epidermal hydration | Skin hydration measured by Corneometer | Twenty-four weeks | No |
Secondary | Change from baseline in skin barrier integrity | TEWL measured by Tewameter | Tewnty-four weeks | No |
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